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Bryan W Reutter

Publications and source records attributed to Bryan W Reutter.

3 recordsLinked to original sources

Method of generating multiple sets of experimental phantom data.

UNLABELLED: Currently, 2 types of phantoms (physical and computer generated) are used for testing and comparing tomographic reconstruction methods. Data from physical phantoms include all physical effects associated with the detection of radiation. However, with physical phantoms it is difficult to control the number of detected counts, simulate the dynamics of uptake and washout, or create multiple noise realizations of an acquisition. Computer-generated phantoms can overcome some of the disadvantages of physical phantoms, but simulation of all factors affecting the detection of radiation is extremely complex and in some cases impossible. To overcome the problems with both types of phantoms, we developed a physical and computer-generated hybrid phantom that allows the creation of multiple noise realizations of tomographic datasets of the dynamic uptake governed by kinetic models. METHODS: The method is phantom and camera specific. We applied it to an anthropomorphic torso phantom with a cardiac insert, using a SPECT system with attenuation correction. First, real data were acquired. For each compartment (heart, blood pool, liver, and background) of the physical phantom, large numbers of short tomographic projections were acquired separately for each angle. Sinograms were built from a database of projections by summing the projections of each compartment of the phantom. The amount of activity in each phantom compartment was regulated by the number of added projections. Sinograms corresponding to various projection times, configurations and numbers of detector heads, numbers of noise realizations, numbers of phantom compartments, and compartment-specific time-activity curves in MBq/cm3 were assembled from the database. RESULTS: The acquisition produced a database of 120 projection angles ranging over 360 degrees . For each angle, 300 projections of 0.5 s each were stored in 128 x 128 matrices for easy access. The acquired database was successful in the generation of static and dynamic sinograms for which the myocardial uptake and washout was governed by a compartment kinetic model. CONCLUSION: A method has been developed that allows creation of sinograms of physical phantoms with the capacity to control the number of noise realizations, the level of noise, the dynamics of uptake in the phantom compartments, and the acquisition parameters and acquisition modes.

Algorithms↗

Kinetic analysis of 18F-fluorodihydrorotenone as a deposited myocardial flow tracer: comparison to 201Tl.

UNLABELLED: The goals of this investigation were to assess the accuracy of (18)F-fluorodihydrorotenone ((18)F-FDHR) as a new deposited myocardial flow tracer and to compare the results to those for (201)Tl. METHODS: The kinetics of these flow tracers in 22 isolated, erythrocyte- and albumin-perfused rabbit hearts were evaluated over a flow range encountered in patients. The 2 flow tracers plus a vascular reference tracer ((131)I-albumin) were introduced as a bolus through a port just above the aortic cannula. Myocardial extraction, retention, washout, and uptake parameters were computed from the venous outflow curves with the multiple-indicator dilution technique and spectral analysis. RESULTS: The mean +/- SD initial extraction fractions for (18)F-FDHR (0.85 +/- 0.07) and (201)Tl (0.87 +/- 0.05) were not significantly different, although the initial extraction fraction for (18)F-FDHR declined with flow (P < 0.0001), whereas the initial extraction fraction for (201)Tl did not. The washout of (201)Tl was faster (P < 0.001) and more affected by flow (P < 0.05) than was the washout of (18)F-FDHR. Except for the initial extraction fraction, (18)F-FDHR retention was higher (P < 0.001) and less affected by flow (P < 0.05) than was (201)Tl retention. Reflecting its superior retention, the net uptake of (18)F-FDHR was better correlated with flow than was that of (201)Tl at both 1 and 15 min after tracer introduction (P < 0.0001 for both comparisons). CONCLUSION: The superior correlation of (18)F-FDHR uptake with flow indicates that it is a better flow tracer than (201)Tl in the isolated rabbit heart. Compared with the other currently available positron-emitting flow tracers ((82)Rb, (13)N-ammonia, and (15)O-water), (18)F-FDHR has the potential of providing excellent image resolution without the need for an on-site cyclotron.

Animals↗

Flow heterogeneity following global no-flow ischemia in isolated rabbit heart.

The purpose of this study was to evaluate flow heterogeneity and impaired reflow during reperfusion after 60-min global no-flow ischemia in the isolated rabbit heart. Radiolabeled microspheres were used to measure relative flow in small left ventricular (LV) segments in five ischemia + reperfused hearts and in five nonischemic controls. Relative flow heterogeneity was expressed as relative dispersion (RD) and computed as standard deviation/mean. In postischemic vs. preischemic hearts, RD was increased for the whole LV (0.92 +/- 0.41 vs. 0.37 +/- 0.07, P < 0.05) as well as the subendocardium (Endo) and subepicardium considered separately (1.28 +/- 0.74 vs. 0.30 +/- 0.09 and 0.69 +/- 0.22 vs. 0.38 +/- 0.08; P < 0.05 for both comparisons, respectively) during early reperfusion. During late reperfusion, the increased RD for the whole LV and Endo remained significant (0.70 +/- 0.22 vs. 0.37 +/- 0.07 and 1.06 +/- 0.55 vs. 0.30 +/- 0.09; P < 0.05 for both comparisons, respectively). In addition to the increase in postischemic flow heterogeneity, there were some regions demonstrating severely impaired reflow, indicating that regional ischemia can persist despite restoration of normal global flow. Also, the relationship between regional and global flow was altered by the increased postischemic flow heterogeneity, substantially reducing the significance of measured global LV reflow. These observations emphasize the need to quantify regional flow during reperfusion after sustained no-flow ischemia in the isolated rabbit heart.

Animals↗